Canonical Allele Identifier: CA916124067
Gene: PLA2G2A HGNC NCBI

Linked Data

dbSNP Id: rs1571226311

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19978561_19978562insCAGAGA , CM000663.2:g.19978561_19978562insCAGAGA GRCh38
NC_000001.10:g.20305054_20305055insCAGAGA , CM000663.1:g.20305054_20305055insCAGAGA GRCh37
NC_000001.9:g.20177641_20177642insCAGAGA NCBI36
NG_012928.1:g.6879_6880insCTCTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000482011.3:c.41-37_41-36insCTCTGT MANE Select ENSP00000504762.1:n.41-37_41-36insCTCTGT
ENST00000400520.8:c.41-37_41-36insCTCTGT ENSP00000383364.3:n.41-37_41-36insCTCTGT
ENST00000482011.2:c.41-37_41-36insCTCTGT ENSP00000504762.1:n.41-37_41-36insCTCTGT
ENST00000649436.1:c.-1-77_-1-76insCTCTGT ENSP00000496912.1:n.-1-77_-1-76insCTCTGT
ENST00000375111.7:c.41-37_41-36insCTCTGT ENSP00000364252.3:n.41-37_41-36insCTCTGT
ENST00000400520.7:c.41-37_41-36insCTCTGT ENSP00000383364.3:n.41-37_41-36insCTCTGT
ENST00000461140.1:n.335-77_335-76insCTCTGT
ENST00000469162.5:n.207-37_207-36insCTCTGT
ENST00000482011.1:n.313-37_313-36insCTCTGT
ENST00000491964.5:n.273-37_273-36insCTCTGT
ENST00000496748.1:n.354_355insCTCTGT
NM_000300.3:c.41-37_41-36insCTCTGT NP_000291.1:n.41-37_41-36insCTCTGT
NM_001161727.1:c.41-37_41-36insCTCTGT NP_001155199.1:n.41-37_41-36insCTCTGT
NM_001161728.1:c.41-37_41-36insCTCTGT NP_001155200.1:n.41-37_41-36insCTCTGT
NM_001161729.1:c.41-37_41-36insCTCTGT NP_001155201.1:n.41-37_41-36insCTCTGT
NM_000300.4:c.41-37_41-36insCTCTGT NP_000291.1:n.41-37_41-36insCTCTGT
NM_001161727.2:c.41-37_41-36insCTCTGT NP_001155199.1:n.41-37_41-36insCTCTGT
NM_001161728.2:c.41-37_41-36insCTCTGT NP_001155200.1:n.41-37_41-36insCTCTGT
NM_001395463.1:c.41-37_41-36insCTCTGT MANE Select NP_001382392.1:n.41-37_41-36insCTCTGT